H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA
H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA Basic information
- Product Name:
- H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA
- Synonyms:
-
- H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA
- L-Argininamide, L-tryptophyl-L-phenylalanyl-L-tyrosyl-O-phosphono-L-seryl-L-prolyl-N-(4-nitrophenyl)- (9CI)
- H-Trp-Phe-Tyr-Ser(PO3H2)-Pro-Arg-pNA trifluoroacetate salt
- H-Trp-Phe-Tyr-Ser(PO?H?)-Pro-Arg-pNA
- CAS:
- 202739-41-1
- MF:
- C49H59N12O13P
- MW:
- 1055.04
- Mol File:
- Mol File
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H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA Chemical Properties
- Density
- 1.53±0.1 g/cm3(Predicted)
- storage temp.
- -15°C
- pka
- 1.80±0.10(Predicted)
- Sequence
- Trp-Phe-Tyr-{PO2}-Ser-Pro-Arg
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H-TRP-PHE-TYR-SER(PO3H2)-PRO-ARG-PNA Usage And Synthesis
Uses
H-Trp-Phe-Tyr-Ser(PO3H2)-Pro-Arg-pNA is a chromogenic substrate for Pin1. Pin1 is an essential and conserved mitotic peptidyl-prolyl isomerase, and can recognize the phosphoserine-proline bonds present in mitotic phosphoproteins[1][2].
References
[1] M B Yaffe, et al. Sequence-specific and phosphorylation-dependent proline isomerization: a potential mitotic regulatory mechanism. Science. 1997 Dec 12;278(5345):1957-60. DOI:10.1126/science.278.5345.1957
[2] Kelly E Duncan, et al. Discovery and characterization of a nonphosphorylated cyclic peptide inhibitor of the peptidylprolyl isomerase, Pin1. J Med Chem. 2011 Jun 9;54(11):3854-65. DOI:10.1021/jm200156c
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